Canonical Allele Identifier: PA916039675
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser652Arg
CA10578330
NM_001354896.2:c.1956T>G
CA16025473
NM_001354896.2:c.1954A>C
CA16025479
NM_001354896.2:c.1956T>A